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In 1991, the National Task Force on Health Information cited a number of issues and problems with the health information system. To respond to these issues, the Canadian Institute for Health Information (CIHI), Statistics Canada and Health Canada joined forces to create a Health Information Roadmap. From this mandate, the Canadian Community Health Survey (CCHS) was conceived. The CCHS is a cross-sectional survey that collects information related to health status, health care utilization and health determinants for the Canadian population. The survey is offered in both official languages. It relies upon a large sample of respondents and is designed to provide reliable estimates at the health region level every 2 years. The CCHS has the following objectives: - Support health surveillance programs by providing health data at the national, provincial and intra-provincial levels; - Provide a single data source for health research on small populations and rare characteristics; - Timely release of information easily accessible to a diverse community of users; - Create a flexible survey instrument that includes a rapid response option to address emerging issues related to the health of the population. The CCHS produces an annual microdata file and a file combining two years of data. The CCHS collection years can also be combined by users to examine populations or rare characteristics. The primary use of the CCHS data is for health surveillance and population health research. Federal and provincial departments of health and human resources, social service agencies, and other types of government agencies use the information collected from respondents to monitor, plan, implement and evaluate programs to improve the health of Canadians. Researchers from various fields use the information to conduct research to improve health. Non-profit health organizations and the media use the CCHS results to raise awareness about health, an issue of concern to all Canadians. The survey began collecting data in 2001 and was repeated every two years until 2005. Starting in 2007, data for the Canadian Community Health Survey (CCHS) were collected annually instead of every two years. While a sample of approximately 130,000 respondents were interviewed during the reference periods of 2001, 2003 and 2005, the sample size was changed to 65,000 respondents each year starting in 2007. In 2012, CCHS began work on a major redesign project that was completed and implemented for the 2015 cycle. The objectives of the redesign were to review the sampling methodology, adopt a new sample frame, modernize the content and review the target population. Consultations were held with federal, provincial and territorial share partners, health region authorities and academics. As a result of the redesign, the current CCHS has a new collection strategy, is drawing the sample from two different frames and has undergone major content revisions. With all these factors taken together, caution should be taken when comparing data from previous cycles to data released for the 2015 cycle onwards.
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In 1991, the National Task Force on Health Information cited a number of issues and problems with the health information system. To respond to these issues, the Canadian Institute for Health Information (CIHI), Statistics Canada and Health Canada joined forces to create a Health Information Roadmap. From this mandate, the Canadian Community Health Survey (CCHS) was conceived. The CCHS is a cross-sectional survey that collects information related to health status, health care utilization and health determinants for the Canadian population. The survey is offered in both official languages. It relies upon a large sample of respondents and is designed to provide reliable estimates at the health region level every 2 years. The primary use of the CCHS data is for health surveillance and population health research. The data presented here is by age group and sex, for Canada, provinces, territories and health regions (2017 boundaries).
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Human biomonitoring is used to estimate exposure to environmental chemicals by measuring the chemical, its metabolites, or reaction products in biological specimens. Since 2007, the biomonitoring component of the Canadian Health Measures Survey (CHMS) has measured hundreds of chemicals in blood, urine, hair, or pooled serum. The CHMS is an ongoing national survey with data collected in two-year cycles. Biomonitoring data are available through an interactive online tool called the Canadian Biomonitoring Dashboard (https://health-infobase.canada.ca/biomonitoring/). New data will be added to the dashboard as they become available. Information specific to the biomonitoring component of the CHMS, including general information on the survey design, fieldwork, laboratory and statistical analyses, and considerations for data interpretation can be found in Health Canada’s biomonitoring reports. These archived reports as well as biomonitoring resources such as a biomonitoring content summary and fact sheets are available on the Resources (https://health-infobase.canada.ca/biomonitoring/resources.html) tab of the Canadian Biomonitoring Dashboard. More information on the full survey can be found on the Statistics Canada website (https://www.statcan.gc.ca/en/survey/household/5071).
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TwitterThis table describes the proportion of the population with select underlying health conditions that are believed to increase the risk of negative outcomes following COVID-19 infection, including hospitalization and death. Estimates are based on data from the 2017-2018 Canadian Community Health Survey, and are provided for the Canadian adult (age 18 and older) population by sex, age and region of residence.
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TwitterUnemployment rate of Canadians aged 15 to 24 and 15 and over, Canada, provinces and territories, health regions and peer groups.
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In 1991, the National Task Force on Health Information cited a number of issues and problems with the health information system. To respond to these issues, the Canadian Institute for Health Information (CIHI), Statistics Canada and Health Canada joined forces to create a Health Information Roadmap. From this mandate, the Canadian Community Health Survey (CCHS) was conceived. The CCHS is a cross-sectional survey that collects information related to health status, health care utilization and health determinants for the Canadian population. The survey is offered in both official languages. It relies upon a large sample of respondents and is designed to provide reliable estimates at the health region level every 2 years. The primary use of the CCHS data is for health surveillance and population health research. The data presented here is by age group and sex, for Canada, provinces, territories and health regions (2017 boundaries).
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TwitterThis survey shows the percentage of Canadians over the age of 65 years with cost barriers to accessing health care in 2017, by income group. In that year, around eight percent of those with a household income of less than 25,000 Canadian dollars had problems or were unable to pay medical bills in the past 12 months.
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This dataset includes statistics on injuries for all ages. The information is from the electronic database of the Canadian Hospitals Injury Reporting and Prevention Program (eCHIRPP) for the year 2017.
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TwitterThis statistic shows the per capita health care spending in the United States, Canada and Germany from 2010 to 2017. In 2017, per capita health care spending in the U.S. stood at 10,209 U.S. dollars. That was more than twice as much as per capita spending in Canada.
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TwitterHousehold food security status, by living arrangement, Canada, provinces and territories.
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The Canadian health insurance system is achieved through 13 interlocking provincial and territorial health care insurance plans, and is designed to ensure that all eligible residents of Canadian provinces and territories have reasonable access to medically necessary hospital and physician services on a prepaid basis, without charges related to the provision of insured health services.
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Canada CA: Proportion of Population Spending More Than 10% of Household Consumption or Income on Out-of-Pocket Health Care Expenditure: % data was reported at 3.500 % in 2019. This records a decrease from the previous number of 3.800 % for 2017. Canada CA: Proportion of Population Spending More Than 10% of Household Consumption or Income on Out-of-Pocket Health Care Expenditure: % data is updated yearly, averaging 3.500 % from Dec 2000 (Median) to 2019, with 15 observations. The data reached an all-time high of 4.400 % in 2009 and a record low of 2.900 % in 2001. Canada CA: Proportion of Population Spending More Than 10% of Household Consumption or Income on Out-of-Pocket Health Care Expenditure: % data remains active status in CEIC and is reported by World Bank. The data is categorized under Global Database’s Canada – Table CA.World Bank.WDI: Social: Poverty and Inequality. Proportion of population spending more than 10% of household consumption or income on out-of-pocket health care expenditure. Out-of-pocket health expenditure is defined as any spending incurred by a household when any member uses a health good or service to receive any type of care (preventive, curative, rehabilitative, long-term or palliative care); provided by any type of provider; for any type of disease, illness or health condition; in any type of setting (outpatient, inpatient, at home).;Global Health Observatory. Geneva: World Health Organization; 2023. (https://www.who.int/data/gho/data/themes/topics/financial-protection);Weighted average;This is the Sustainable Development Goal indicator 3.8.2[https://unstats.un.org/sdgs/metadata/].
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Canada sa: FI: Life, Health & Medical Insurance Carrier data was reported at 2,305.000 CAD mn in Dec 2022. This records an increase from the previous number of 1,384.000 CAD mn for Sep 2022. Canada sa: FI: Life, Health & Medical Insurance Carrier data is updated quarterly, averaging 1,875.000 CAD mn from Mar 2020 (Median) to Dec 2022, with 12 observations. The data reached an all-time high of 3,090.000 CAD mn in Jun 2022 and a record low of 291.000 CAD mn in Mar 2020. Canada sa: FI: Life, Health & Medical Insurance Carrier data remains active status in CEIC and is reported by Statistics Canada. The data is categorized under Global Database’s Canada – Table CA.O012: CSMA: Corporate Net Income Before Taxes: NAICS 2017.
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This driver represents total public and private health expenditure in Canada. Data is presented in 2017 dollar terms and is sourced from the Canadian Institute for Health Information.
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TwitterIn the period 2017 to 2020, it was found that around 66 percent of Inuits in Canada aged 18 to 34 years did not have a regular health care provider. In comparison, 25 percent of non-indigenous people in this age group did not have a regular health care provider. This statistic shows the percentage of First Nations people living off reserve, Métis, Inuit and non-Indigenous people in Canada without a regular health care provider between 2017 and 2020, by age.
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Cancer incidence, by selected sites of cancer and sex, three-year average, Canada, provinces, territories and health regions (2017 boundaries)
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TwitterAs the COVID-19 pandemic spreads, researchers and health professionals have noted large differences in the impact that the infection has on individuals. Whereas some remain asymptomatic and unaware of their infection or experience only mild symptoms, others require hospitalization, ventilation, and may even die. As research evidence accumulates, both nationally and internationally, it appears that certain health characteristics, such as obesity or the presence of chronic conditions, increase the risk of severe outcomes among those who are infected with the novel coronavirus. To better understand which segments of the Canadian population may be vulnerable to severe health outcomes related to COVID-19, Statistics Canada and the Public Health Agency of Canada have worked collaboratively to build an index of underlying health conditions in the adult household population. Using information from the 2017/2018 Canadian Community Health Survey, new data tables released today estimate the proportion of the adult household population who may be at greater risk of severe health outcomes related to COVID-19 due to the presence of underlying health conditions.
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Census indicator profile, based on the 2016 Census long-form questionnaire, Canada, provinces and territories, and health regions.
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TwitterEstimated number of persons on July 1st, by age group and sex, for Canada, provinces and territories, health regions and peer groups.
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TwitterRank, number of deaths, percentage of deaths, and age-specific mortality rates for the leading causes of death, by age group and sex, 2000 to most recent year.
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In 1991, the National Task Force on Health Information cited a number of issues and problems with the health information system. To respond to these issues, the Canadian Institute for Health Information (CIHI), Statistics Canada and Health Canada joined forces to create a Health Information Roadmap. From this mandate, the Canadian Community Health Survey (CCHS) was conceived. The CCHS is a cross-sectional survey that collects information related to health status, health care utilization and health determinants for the Canadian population. The survey is offered in both official languages. It relies upon a large sample of respondents and is designed to provide reliable estimates at the health region level every 2 years. The CCHS has the following objectives: - Support health surveillance programs by providing health data at the national, provincial and intra-provincial levels; - Provide a single data source for health research on small populations and rare characteristics; - Timely release of information easily accessible to a diverse community of users; - Create a flexible survey instrument that includes a rapid response option to address emerging issues related to the health of the population. The CCHS produces an annual microdata file and a file combining two years of data. The CCHS collection years can also be combined by users to examine populations or rare characteristics. The primary use of the CCHS data is for health surveillance and population health research. Federal and provincial departments of health and human resources, social service agencies, and other types of government agencies use the information collected from respondents to monitor, plan, implement and evaluate programs to improve the health of Canadians. Researchers from various fields use the information to conduct research to improve health. Non-profit health organizations and the media use the CCHS results to raise awareness about health, an issue of concern to all Canadians. The survey began collecting data in 2001 and was repeated every two years until 2005. Starting in 2007, data for the Canadian Community Health Survey (CCHS) were collected annually instead of every two years. While a sample of approximately 130,000 respondents were interviewed during the reference periods of 2001, 2003 and 2005, the sample size was changed to 65,000 respondents each year starting in 2007. In 2012, CCHS began work on a major redesign project that was completed and implemented for the 2015 cycle. The objectives of the redesign were to review the sampling methodology, adopt a new sample frame, modernize the content and review the target population. Consultations were held with federal, provincial and territorial share partners, health region authorities and academics. As a result of the redesign, the current CCHS has a new collection strategy, is drawing the sample from two different frames and has undergone major content revisions. With all these factors taken together, caution should be taken when comparing data from previous cycles to data released for the 2015 cycle onwards.